Nabais Sá, Maria J.
Jensik, Philip J.
McGee, Stacey R.
Parker, Michael J.
Lahiri, Nayana
McNeil, Evan P.
Kroes, Hester Y.
Hagerman, Randi J.
Harrison, Rachel E.
Montgomery, Tara
Splitt, Miranda
Palmer, Elizabeth E.
Sachdev, Rani K.
Mefford, Heather C.
Scott, Abbey A.
Martinez-Agosto, Julian A.
Lorenz, Rüdiger
Orenstein, Naama
Berg, Jonathan N.
Amiel, Jeanne
Heron, Delphine
Keren, Boris
Cobben, Jan-Maarten
Menke, Leonie A.
Marco, Elysa J.
Graham, John M. Jr
Pierson, Tyler Mark
Karimiani, Ehsan Ghayoor
Maroofian, Reza
Manzini, M. Chiara
Cauley, Edmund S.
Colombo, Roberto
Odent, Sylvie
Dubourg, Christele
Phornphutkul, Chanika
de Brouwer, Arjan P.M.
de Vries, Bert B.A.
Vulto-vanSilfhout, Anneke T.
This article is maintained by: Elsevier
Article Title: De novo and biallelic DEAF1 variants cause a phenotypic spectrum
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0473-6
Content Type: article
Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics